• Quality Manager

    WestRock Company (East Flat Rock, NC)
    …procedures. You will support introduction of new equipment on site and validation processes to meet safety and customer expectations. Additionally, you will promote ... * Bachelor\u2019s Degree is preferred, ASQ certification is a plus * Pharmaceutical Printing and / or Packaging industry experience is preferred * Ability… more
    WestRock Company (08/21/25)
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  • Associate Director - Site Systems and Compliance

    Lilly (Lebanon, IN)
    …to drive business process optimization. + Adhere to corporate computer systems validation policies and procedures. + Progress the digital roadmap at the Lilly ... + Minimum of (8) years' experience in manufacturing, preferred in pharmaceutical or other regulated industries. + Experience with integrated business process… more
    Lilly (08/21/25)
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  • Research Scientist II; Analytical Development

    Curia (Albany, NY)
    …Curia provides global contract research and manufacturing services to the pharmaceutical and biotechnology industries. The Analytical Department is responsible for ... * Write analytical method procedures to establish format * Write analytical validation reports * Develop new procedures for new compounds * Process samples… more
    Curia (08/21/25)
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  • Manager, Nonclinical Safety US, Experimental…

    Boehringer Ingelheim (Ridgefield, CT)
    …for all study activities (tissue trimming through archiving), serving as the validation manager for all equipment and software used in the laboratory, as ... expected. + Understanding of toxicology principles and testing programs in the pharmaceutical industry is desirable. + Strict attention to detail and follow-up… more
    Boehringer Ingelheim (08/21/25)
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  • Information Systems, R&D Commercialization…

    Amgen (Washington, DC)
    …platforms and enterprise systems. + Manage UAT planning, test case validation , and production deployment oversight. + Partner closely with cross-functional teams, ... or Agile/Scrum frameworks. + Background in life sciences, biotechnology, or pharmaceutical R&D. + Understanding of the drug development lifecycle and relevant… more
    Amgen (08/21/25)
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  • Sr. Principal MES Advisor - TS/MS - Lebanon API…

    Lilly (Lebanon, IN)
    …skills, complex problem-solving abilities. + Strong knowledge of pharmaceutical manufacturing processes, facility start-up procedures, and GMP regulations. ... + Previous experience supporting cGMP manufacturing within Operations, Validation , Engineering, Technical Services/MSAT, Quality Assurance, etc. + Prior experience… more
    Lilly (08/20/25)
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  • Systems Engineer

    Kelly Services (Haverhill, MA)
    …lack of data, or new market requirements. Coordinate testing plans between validation and verification testing. Ensure testing of customer usage cases to evaluate ... including power, glass and other coating applications; steel and other metallurgy; pharmaceutical and chemical; and for scientific instruments in a wide range of… more
    Kelly Services (08/20/25)
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  • R&D Programmer

    Kelly Services (PA)
    …strong programming support to CDISC based e-submission. Develop, review, and/or perform validation of generic macros. + Develop, debug, and enhance SAS programs to ... + 5 years or Master's + 4 years of professional experience in a pharmaceutical or clinical research setting as a programmer **Experience Preferred:** + Experience in… more
    Kelly Services (08/20/25)
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  • Manufacturing Supervisor- Blood Components

    American Red Cross (Nashville, TN)
    …Lead suspect product/sample management process. + May participate in the validation of hardware, software, instrumentation, test kits, and procedures as directed. ... substituted). + Education: Bachelor's degree is a plus + Blood Bank or Pharmaceutical manufacturing experience is a plus. _BENEFITS FOR YOU:_ As a mission-based… more
    American Red Cross (08/19/25)
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  • Quality Assurance Associate (FDA Regulatory)

    Family Dollar (Chesapeake, VA)
    …and maintaining an Approved Supplier List. + Assure that appropriate process validation and stability studies are conducted and retain samples are maintained to ... + Minimum 3 years of Quality work experience in FDA regulated industries. ( pharmaceutical or medical device industry preferred). + Working knowledge of FDA Quality… more
    Family Dollar (08/19/25)
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